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Variant : CV604029 (GRCh37/hg19 1q32.1(chr1:201952244-201959490)x3) Homo sapiens

Symbol: CV604029
Name: GRCh37/hg19 1q32.1(chr1:201952244-201959490)x3
Condition: not provided [RCV000749329]
Clinical Significance: benign
Last Evaluated: 11/19/2010
Review Status: no assertion criteria provided
Related Genes: RNPEP  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371201,952,244 - 201,959,490CLINVAR
Cytogenetic Map11q32.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14364660
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-21
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.